Polymer stabilization with 1, 4, 7, 9beta-tetraazaphenalene compounds



United States Patent 3,397,167 POLYMER STABILIZATION WITH 1,4,7,9b-TETRA- AZAPHENALENE COMPOUNDS Jerry T. Gruver, Bartlesville, 0lrla., assignor to Phillips Petroleum Company, a corporation of Delaware No Drawing. Filed June 29, 1964, Ser. No. 378,938 9 Claims. (Cl. 26033.6)

ABSTRACT OF THE DISCLOSURE Stabilization of polymers including carbon black containing rubbers with 1,4,7,9b-tetraazaphenalene compounds as antioxidants.

This invention relates to the stabilization of polymeric materials. In accordance with another aspect, this invention relates to polymeric compositions containing carbon black subject to oxidative degradation stabilized against such degradation by the addition thereto of certain tetraazaphenalenes. In accordance with another aspect, this invention relates to a method for inhibiting oxidation of polymeric materials by incorporating therein a stabilizing amount of a tetraazaphenalene compound. In accordance with a further aspect, this invention relates to the stabilization of polymeric materials containing carbon black and extender oils by the addition thereto of a tetraazaphenalene compound. In accordance with a further aspect, this invention relates to the stabilization of polymeric materials containing a high percentage of cis-1,4-addition by incorporating therein a stabilizing amount of a tetraazaphenalene compound. In accordance with still a further aspect, this invention relates to the preservation of cis-polybutadiene-carbon black masterbatches by incorporating therein a tetraazaphenalene compound.

Natural and synthetic rubbers, as well as polyolefins, are subject to oxidative degradation when exposed to an oxygen-containing atmosphere, particularly at elevated temperatures and/ or in the presence of actinic light. This oxidative degradation is accelerated by the presence of reinforcing agents, such as carbon black, in polymeric masterbatches. Such degradation results in loss of processability, ernbrittlement, loss of tensile strength and elongation, detrimental color changes, decrease in inherent viscosity, increase in percentage gel, decrease in swelling index, and the like. Thus, it can be seen that there is a general deterioration in the physical properties of such polymers. Numerous additives have been proposed for inhibiting such oxidative degradation, most of which, while possibly effective for some compositions, have many shortcomings. US. Patents 2,388,562, A. M. Neal et al., issued Nov. 6, 1945, Re. 19,654, M. C. Reed, reissued July 23, 1935, and 2,705,224, E. L. Hill et al., issued Mar. 29, 1955, all disclose various aromatic amines as rubber antioxidants and antioxidants. Because of the presence of reinforcing agents, such as carbon black in many polymer compositions, the shortcomings of some known inhibitors are especially apparent in attempting to prevent or slow down oxidative degradation of polymericcarbon black masterbatches.

The present invention relates to novel antioxidants which are highly eifective in stabilizing polymers subject to oxidative degradation against oxidative degradation.

Accordingly, an object of this invention is to provide polymeric materials stabilized against oxidation.

Another object of this invention is to provide a method for stabilizing polymers such as natural and synthetic rubbers and polyolefins against oxidative degradation.

Another object of this invention is to provide new compositions of matter and to advance the polymer art.

Still another object of this invention is to provide novel 3,397,167 Patented Aug. 13, 1968 antioxidants for stabilizing polymers containing carbon black subject to oxidative degradation.

7 Other objects, aspects, as well as the several advantages of this invention, will become apparent to those skilled in the art upon a study of this disclosure and the appended claims.

In accordance with present invention it has now been found that polymers subject to oxidative degradation can be stabilized against such degradation by incorporating therein a stabilizing amount of certain tetraazaphenalene compounds.

More specifically, in accordance with the present invention, it has been found that polymers such as natural rubber and solid and rubbery synthetic polymers formed by polymerizing monomers containing a vinylidene group (H C=C can be stabilized against oxidative degradation by incorporating therein a stabilizing amount of a 1,4,7,9b-tetraazaphenalene compound having the structural formula:

wherein R is hydrogen or a monovalent hydrocarbon radical selected from saturated aliphatic, saturated cycloaliphatic, and aromatic radicals, containing up to and including 12 carbon atoms. In the above formula hydrocarbon radicals containing from 1 to 8 carbon atoms, inclusive, are presently preferred.

Representative examples of suitable 1,4,7,9b-tetraazaphenalenes that can be used as antioxidants according to the invention include:

Dodecahydro-1,4,7,9b-tetraazaphenalene, 2,5,S-trimethyldodecahydro-1,4,7,9b-tetraazaphenalene, 2,5,8-triiosobutyldodecahydro-1,4,7,9b-tetraazaphenalene, 2,5,8-triphenyldodecahydro-1,4,7,9b-tetraazaphenalene, 3,6,9-triethyldodecahydro-1,4,7,9b-tetraazaphenalene, 3,6,9-tricyclopentyldodecahydro-1,4,7,9b-tetraazaphenalene, 2,3-diethyldodecahydro-1,4,7,9b-tetraazaphenalene, 3-n-butyldodecahydro-1,4,7,9b-tetraazaphenalene, 2,6-di-n-hexyldodecahydro-1,4,7,9b-tetraazaphenalene, 3,6,9-tri-tert-octyldodecahydro-l,4,7,9b-tetraazaphenalene,

2,5 -dirnethyl-9-isopropyldodecahydro-l,4,7,9b-tetraazaphenalene,

3,6-dibenzyldodecahydro-1,4,7,9b-tetraazaphenalene,

3 (Z-phenylethyl)dodecahydro-1,4,7,9b-tetraazaphenalene,

2,6-di(4-methylcyclohexyl)dodecahydro-1,4,7,9b-tetraazaphenalene,

3 (4-tolyl) dodecahydro-1,4,7,9b-tetraazaphenalene,

2,5-di(2,3-dimethylhexyl) -dodecahydro-1,4,7,9b-tetraazaphenalene,

2(2,6-diethylphenyl)dodecahydro-1,4,7,9b-tetraazaphenalene,

2,3,5,6,8,9-hexamethyldodecahydro-1,4,7,9b-tetraazaphenalene,

2,5 -diethyl-3,6-di-n-butyldodecahydro-1,4,7,9b-tetraazaphenalene,

3,6-di-n-propyl-9-phenyldodecahydro-1,4,7,9b-tetraazaphenalene, 3-n-dodecyl-1,4,7,9b-tetraazaphenalene,

and the like.

The stabilizers or antioxidants of the invention can be incorporated into the polymer to be stabilized in any desired amount depending upon the conditions under which the polymer is to be used. However, the total amount of stabilizer required to produce the desired stabilizing effect has been found to be relatively small and will generally range from 2 to 20 millimols per 100 weight parts of polymer, with the preferred amount being in the range of 4 to millimols per 100 weight parts of polymer.

The tetraazaphenalene compounds employed as stabilizers according to the invention can be prepared by any method known in the art. Also, the stabilizers of the invention can be incorporated into the polymer to be stabilized by any suitable means, such as hot milling in a roll mill or hot mixing in a Banbury mixer, solution-blending, and the like.

The materials that can be stabilized according to the invention include, in general, polymeric materials that are subject to oxidative degradation. Preferably, the polymeric materials that can be stabilized according to the invention include natural rubber and synthetic polymers formed from conjugated dienes and monoolefins containing carbon black.

The preferred class of polymers stabilized according to the invention include both homopolymers and copolymers of conjugated dienes having from 4 to 12 carbon atoms, preferably conjugated dienes having from 4 to 8 carbon atoms per molecule such as 1,3-butadiene, isoprene, piperylene, methylpentadiene, 2-methyl-l,3-hexadiene, phenylbutadiene, 3,4-dimethyl-1,3-hexadiene, 4,5-diethyl-l,3- octadiene, and the like. Among these butadiene, isoprene, and piperylene are preferred. In addition, suitable polymeric materials that can be stabilized include copolymers of the above-mentioned conjugated diene with compounds containing a vinylidene group (H C=C such as isobutylene, styrene, p-methoxystyrene, vinylnaphthalene, vinyltoluene heterocyclic nitrogen-containing monomers such as pyridine and quinoline derivatives containing at least one vinyl or alpha-methylvinyl group, such as 2- vinylpyridine and 2-methyl-5-vinylpyridine, acrylic and alkacrylic acid esters, such as methyl acrylate, ethyl acrylate, and methyl methylacrylate, methyl vinyl ether, vinyl chloride, vinylidene chloride, and the like.

The antioxidants of the invention can also be used to stabilize polymers of monoolefins having from 2 to 8 carbon atoms such as polyethylene, polypropylene, polybutene, copolymers of ethylene with propylene, l-butene, and the like. These synthetic polymers of monomers containing a vinylidene group (H C=C can be made by a number of well known processes. Emulsion polymerization of butadicne and vinylidene-containing monomers such as styrene and the vinylpyridines, for example, is a well established process. Mass or solution polymerization employing various catalyst systems are likewise known methods of preparing polymers of mono and diolefins, for example, polyethylene, polypropylene, polybutadiene, polyisoprene, ethylene-propylene rubber, ethylene-propylene terpolymer rubber, and the like.

As indicated previously, the present invention is preferably applicable to the stabilization of polymeric composi tions subject" to oxidative degradation containing pigments or reinforcing agents such as carbon black. The invention is particularly useful in stabilizing polymercarbon black masterbatches, including oil-extended masterbatches. The carbon black employed can be any of the types including both channel and furnace black, lamp black, and the like. Where reference is made to carbon black or carbon particles, this term should be understood to include all forms of carbon which have been found effective for reinforcing or light shielding in polymeric materials. The particle size of the carbon black preferably does not exceed about 1000 Angstroms. Although the invention is discussed in terms of carbon black, the teachings of the invention obviously can be practiced with advantage to the incorporation of other prime reinforcing and extended pigments. Other pigments which are obtained as insoluble particulate solids, such as zinc oxide, titanium dioxide, clays, hydrated alumina, precipitated calcium carbonates, and the like, can be used instead of carbon black or together with carbon black when desired.

The amount of pigment or carbon black employed in reinforcing polymeric materials will-vary appreciably depending upon the particular polymeric material being extended. For example, polymers of conjugated dienes can contain up to about 250 weight parts of carbon black per weight parts of polymer and often will contain from 10 to about weight parts per 100 parts of polymer. Polymers of monoolefins often contain small amounts of carbon black for light shielding purposes and the amount of carbon black employed generally will be in the range of from about 0.5 to about 10 weight parts per 100 weight parts of polymer, although amounts outside this range can be employed when desired. It is often preferred to employ from about 1 to about 5 weight parts of carbon black per 100 parts of polymers of monoolefins. Thus, the amount of carbon black employed in polymers applicable according to the invention can range from 0.5 to 250 weight parts per 100 parts of polymer, preferably from 1 to 150 weight parts.

Rubber reinforcing black, or rubber reinforcing carbon black are generic terms and are given to any of a large variety of carbon blacks that are used in the formulation of polymer compositions, which carbon blacks are applicable to masterbatches of the invention. These blacks are available through normal commercial channels in a large variety of trade names and/or type names as easy processing channel black, medium processing channel black, hard processing channel black, high abrasion furnace black, super abrasion furnace black, intermediate super abrasion furnace black, high modulus furnace black, semi-reinforcing black, and others, which are all characterized by their known utility in the compounding of rubber formulations. These blacks differ by the method of preparing them and/or their average particle sizes and their use in rubber formulations is a matter of choice depending upon the particular rubber that one desires to produce. The present invention is particularly directed to the stabilization of polymeric-carbon black masterbatches containing any of the above-described carbon blacks.

The above-described polymeric-carbon black masterbatches can also be oil extended with any of the known rubber extender oils. The oils that can be employed in the present invention are referred to in the art as compatible oils or compatible rubber extending oils. Among the compatible oils are those ordinarily derived from petroleum, although they may be derived from coal tar or other suitable source. Generally, they have a viscosity of about 10 cs. at 210 F. up to more or less solid materials softening at about 100 to 200 F., have a boiling point of at least 300 F. at 10 mm. Hg and have a specific gravity (60/60 F.) of about 0.9 to 1.05. These are primarily higher hydrocarbons and can be vacuum distillates of petroleum as well as extracts and/or rafiinates of such distillates. Also suitable are residues of petroleum distillation operations. Especially suited are extending oils of the type known as highly aromatic oils. The amount of extender oil employed will vary appreciably depending upon the particular polymeric material being extended, but in general the amount of oil will range up to about 100 weight percent of the carbon black present, preferably from about 10 to about 50 weight percent of the carbon black present.

Other materials can be incorporated into the polymers stabilized according to the invention prior to, together with, or subsequent to the addition of the stabilizers of the invention. These include pigments, dyes, other stabilizers, antistatic agents, fillers, softeners, stress cracking inhibitors, vulcanizing agents, vulcanization accelerators, etc.

Polymer samples were dissolved in carbon disulfide to form a solution having 25 grams of polymer per liter of solution. The nfrared spectrum of each of the solutions (percent transmission) was then determined in a conventional infrared spectrometer.

The percent of the total unsaturatlon present as trans 1,4-

The following examples will illustrate the present in- 5 ggg gg fi g ggg s the equation a s: c, w ere e=ex net on co fii i t 11 irention in greater detail but are not to be construed as mols-teennmetersn) ,Emxtmcuon (g igg g f irnit ng the nvent on, tifltelfiieltgisg and ci=oncentatitoit1h(niig%gouble bond/liter).

inwas eermnea e h hlgh C13 polybutadlene used i the masterbatches the extinction coefiicient was 146 (liter-mols g gn i i's gq t at were used in the tests reported in Examples I and 11 v1 wa e g og hg total nnsa cur tion present a s 1,

' u e aecor ing 0 e a ove e net on, usin was P pa e y polymerlzmg butadlene a reactor Y 10 the 11.0 micron band and an extinction coefficient of 203 tern consisting of two parallel trains having three 4,000 g p e e percen o e 0 a1 unsaturation resent as cis 1,4- ganon stln'ed reflctors 111 tram followed y a com was obtained by subtracting the trans 1,4 and 1,2 (vinyl) mon reactor, 113mg th f ll w r determined according to the above procedure from the theoretical unsaturation, assuming one double bond per each C4 Butadiene 1b,/mi 1523 unit in the p y e Toluene I lb./min 1350.0 15 A polybutadiene/black/oilmasterbatch was prepared by Triisobutylaluminum p.h.m 0.63 m lllng together the following ingredients: Iodine p h m 0.186

Parts by weight Titanium tetrachloride p.h.m 0.0563 Hlghmspolybutadiene 100 1 Part per 100 parts of monomer. Philblack 1 60 5 Reaction was initiated at 45 F. and the temperature was Phllnch 5( 20 allowed to rise to about 75 F. Residence time in each of fi l fie tes per-abras on furnace black. the reactors in the parallel trains was 37.4 minutes and y woman extender in the common reactors was 18.7 minutes. After addition T1115 masterbatch was used 111 the tests p r in EX- of 0.43 p.h.r. (parts per 100 parts of rubber) of Cyanox ample SS[2,2 methylene-bis-(4-methyl-6-tert-butylphenol)], a Example I ZQW Q Q antlgxldalnti gi OfhReSm 1 11 1 Dodecahydro-l,4,7,9b-tetraazaphenalene was employed p p gl ifi P f T0511; 2 f to eat an 1g 0 as an antioxidant for a cis-polybutadiene/carbon black/ ShOFtStOP; t e e lent Tom t h g Tiactor was aromatic oil masterbatch. Three masterbatch samples were Steam PP for g g 'y d t f g c1111? 1 and the prepared and tested for oxygen absorption at 100 C. In crumb was waiter-wads 6 Ian (in; ,f each case the masterbatch was milled into a strip about 196mmt P Ybuta 16116 avlnct e 0 Owmg Propertles- 0.03 inch thick and a one-gram portion of the strip was Microstructure, Percent (a) supported on glass wool that was in turn supported on Cis 933 aluminum foil in an oxygen absorption tube. The time Trans a 3 2 required for the absorption of 10 cc. of oxygenat 100 Viny1 35 C. was determined. In the first, second and fifth samples, Inherent Viscosity (1) 2.53 the Q43 pf CY B X SS, 2,2-methylene-bis-(4meth- Gel, percent (2) 0 y yl P n l), that Was Originally added to the polymer was present. In the third and fourth samples 1 th f l s l 0 din a ire cagemade 40 fron i s 0 ii i esh c i ee i d iz li dd ge isas placed in 100 ml. of y q SS was remcfvfxl PY filssolvmg the -p y tt iiu ne coitained 111 a WiEde-mCEu sen g' ct g diene in toluene, precipitating it with methanol, and vacua room em era ure :1 roxima e l ioiiii, the cage Was removed an d the solutiiin was filtered um drymg It at room temperature- Thls Procedure 1'6- through ulg aitrsolrption lge g po g t duced the Cyanox content to 0.04 percent which was con- 0 ill 1C 65 resen 8 resu g fiih ih i diigli 2 1 hfedalia tyge viscometer supported in a 77 F. sldered neghglble- Sample was prepared Wlthout bath. The viscometer was previously calibrated with toluene. arbon black and 011 Results of the tests are shown in The relative viscosity is the ratio of the viscosity of the T b1 I polymer solution to that of toluene. The inherent viscosity is a e TABLE I Antioxidant Sample Hrs. to Absorb Run No. 10 cc. 02 per g.,

Type phr. mhr. cis-PBd /C Black/Oil, Sample Parts by Weight 1.- Amine Ito-94 0.98 5.4 100/60/20 125 2.. 1. 5 6. 8 100/60/20 53 3-. 100 15 4-. 100/60/20 30 100/60/20 33 5 Polybutadieiie.

calculated by dividing the natural logarithm of the relative viscosity by the weight of the soluble portion of the original sample.

Determination of gel was made along with the inherent viscosity determination. The wire cage was calibrated for toluene retention in order to correct the weight of swelled gel and to determine accurately the weight of dry gel. The empty cage was immersed in toluene and then allowed to drain three minutes in a closed wide-mouth, 2-ounce bottle. A piece of folded quarter-inch hardware cloth in the botom of the bottle supported the cage with minimum contact. The bottle containing the cage was weighed to the nearest 0.0 2 gram during a minimum 3 minute draining period after which the cage was withdrawn and the bottle again weighed to the nearest 0.02 grain. The difference in the two weighings is the weight of the cage plus the toluene retained by it, and by subtracting the weight of the empty cage from this value the weight of toluene retention is found, i.e., the cage calibration. In the gel determination, after the cage containing the sample had stood for 24 hours in toluene, the cage was withdrawn from the bottle with the aid of forceps and placed in the 2-ounce bottle. The same procedure was followed for determining the weight of swelled gel as was used for calibration of the cage. The weight of swelled gel was corrected by subtracting the cage calibration.

The data demonstrates the efficiency of dodecahydro- 1,4,7,9b-tetraazaphenalene, an antioxidant of this invention, for stabilizing the cis-polybutadiene masterbatch.

Example II Amine RC-94, dodecahydro l,4,7,9b-tetraazaphenalene, was employed at two levels in Banbury prepared masterbatches. The masterbatches were then aged at F. for periods of 2,4,6, and 8 weeks after which the compounding ingredients were added on the mill. The stocks were cured 30 minutes at 307 F. and physical properties determined. Runs were also made in which Ionol was used instead of Amine R094 and one composition was prepared without antioxidant. Compounding recipes and physical properties of vulcanizates are given in Table II.

TAB LE II Compounding Recipes, Parts by Weight Cis-Polybutadiene 1 100 100 100 100 100 Philblack I 1 70 70 70 70 70 Zinc oxide 3 3 3 3 3 Stearic acid 2 2 2 2 2 Flexarnine 1 1 1 1 1 Philrich 5 1 30 30 30 30 Sulfur 1. 85 1. 85 1. 85 1. 85 1. S5 Santocure NS 3 1. 1. 45 1. 45 1. 45 1. 45 Amine TLC-94 4 0.75 5 1.5 Ionol 0.75 1.5

Physical Properties, Cured 30 Minutes at 307 F.

uXlO, Moles/cc;

Original 1.64 1. 77 1. 71 Aged 2 weeks at 160 1. 66 1.53 1. 46 1. 44 Aged 4 weeks at 160 1. 75 1. 40 1.36 1. 36 Aged 6 weeks at 160 1. 59 1. 36 1. 48 7. 58 Aged 8 weeks at 160 F-.. 1.72 1. 39 1. 26 AT, F.:

Orig'nal 62. 8 5S. 9 60 60. 3 Aged 2 weeks at 160 F-. 62.0 59. 5 63.0 63. 3 69. 6 Aged 4 weeks at 160 F. 67. 4 60. 5 60. 4 68. 8 82. 2 Aged 6 weeks at 160 F" 68.6 61. 7 73 68. 3 83. 9 Aged 8 Weeks at 100 F. 72. 8 62. 7 83 81. 3 Resilience, percent:

Original 65. 1 65.8 66. 3 65. 3 Aged 2 weeks at 160 F- 68. 9 70. 3 66. 3 65.3 65. 6 Aged 4 weeks at 160 F 69. 4 71.2 66. 0 64.8 66. 8 Aged 6 weeks at 160 F" 69.8 71. 2 67.9 67. 3 65. 9 Aged 8 weeks at 160 F 68 69.6 64. 2 64.8 300% Modulus, p.s.i.:

Or inal 1, 070 1, 150 1, 080 1,190 Aged 2 weeks at 160 F 1, 340 1, 360 1, 180 1,100 1, 140 Aged 4 weeks at 160 F 1, 270 1, 360 1,160 1,040 1, 160 Aged 6 weeks at 160 F 1, 120 1, 340 1,070 1,070 1, 170 Aged 8 weeks at 160 F 1,440 1,240 1, 010 Tensile, p.s.i.:

Original 1. 2, 480 2, 550 2,270 2, 390 Aged 2 weeks at 160 F 2, 540 2, 580 2, 380 2, 030 2, 100 Aged 4 weeks at 160 F 2, 320 2, 130 2, 210 2, 425 1, 330 Aged 6 weeks at 160 F. l, 730 2,040 1, 230 Aged 8 weeks at 160 F-- 1, 580 750 Elongation, percent:

riginal 520 510 480 480 Aged 2 weeks at 160 F 480 475 485 460 460 Aged 4 weeks at 160 F 440 400 465 520 325 Aged 6 weeks at 160 F 385 385 410 480 310 Aged 8 weeks at 160 F 265 370 350 420 1 Added during masterbateh preparation.

2 Physical mixture containing percent of a complex diarylamincletone reaction product and 35 percent of N,N-diphenyl-p-phenyleneiamine.

3 N tert-butyl-2-benzothiazolesulfenamide.

4 4.1 mhr.

5 8.2 mhr.

6 3.4 mhr.

7 6.8 mhr.

These data show that aging produced less change in the crosslinking value (vx 10 moles/cc.) when Amine RC-94, an antioxidant, of the invention, was present in the mastcrbatch than when Ionol, a commercial antioxidant was used. Likewise there was less change in heat build-up in the compositions containing Amine RC-94 than in those containing Ionol. The change in resilience was not great but the data show some advantage when Amine RC-94 was used.

Reasonable variation and modification are possible within the scope of the foregoing disclosure and the appended claims to the invention, the essence of which is that polymeric material subject to oxidative degradation are inhibited against such degradation by incorporation therein of certain 1,4,7-9b-tetraazaphenalene compounds.

I claim:

1. A composition of matter of increased stability against oxidative degradation comprising:

(a) a polymer selected from natural rubber and solid polymers of monoolcfins having from 2 to 8 carbon atoms and rubbery synthetic polymers formed by polymerizing conjugated dicnes having 4 to 12 carbon atoms, and

8 (b) a stabilizing amount from 2 to 20 millimoles of (b) per weight parts of (a) of a 1,4,7-9b-tctraazaphenalene compound of the formula:

wherein R is selected from hydrogen and monovalent hydrocarbon radicals selected from saturated aliphatic, saturated cycloaliphatic, and aromatic radicals, and combinations thereof, containing up to and including 12 carbon atoms.

2. A composition according to claim 1 which contains (c) from 0.5 to 250 weight parts carbon black per 100 weight parts of (a).

3. A composition according to claim 2 which contains (d) an extender oil in amounts up to 100 weight percent of the carbon black (0) present in said composition.

4. A composition of matter comprising (a) a rubbery polymer of a conjugated diene having from 4 to 12 carbon atoms per molecule, (b) from about 0.5 to about 250 weight parts carbon black per 100 weight parts of rubber, and (c) from about 2 to about 20 millimols of a stablizing compound having a formula as defined in claim 1.

5. A composition according to claim 4 wherein said rubbery polymer is polybutadiene having a high percentage of cis-1,4-addition.

6. A composition of matter comprising polybutadienc, from 10 to weight parts carbon black per 100 weight parts polybutadiene, from 10 to 50 weight percent of an aromatic extender oil based on carbon black, and from 2 to 20 millimols of dodecahydro-l,4,7,9b-tetraazaphenallene per 100 weight parts polybutadicne.

7. A composition of matter comprising cis-polybutadiene, and per 100 weight parts of cis-polybutadiene, 10- 150 weight parts of carbon black, 10-150 weight percent of a highly aromatic extender oil based on carbon black, and from 4 to 15 millimols of dodccahydro-1,4,6,9b-tetraazaphcnalene.

8. A composition according to claim 6 wherein said polybutadiene contains a high percentage of cis-1,4- addition.

9. A cured rubber composition of matter comprising a high cis-polybutadine, and per 100 weight parts of polybutadicne, 10150 weight parts carbon black, 10-50 weight percent of a highly aromatic extender oil based on carbon black, and from 2 to 20 millimols of dodecahydro-1,4,7,9b-tetraazaphenalene.

References Cited UNITED STATES PATENTS 3,112,315 11/1963 Van Winkle 26O256.4 2,658,895 11/ 1953 Ballard 260-800 2,388,562 11/1945 Neal 260-800 2,705,224 3/1955 Hill 260-285 3,196,126 7/1965 Wald 260-336 3,203,922 8/1965 Hammer 260-33.6

OTHER REFERENCES Shell: Technical Information Bulletin, April 1963, Amine RC-94, pages 1-6, copy in S.L. 260-2564.

Brown: Rubber World, pp. 70-76, November 1961.

JULIUS FROME, Primary Examiner. 

